Fluoxetine
Product Images NDC 42571-387

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Fluoxetine (NDC 42571-387). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Micro Labs Limited, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Fluoxetine-10lbl.jpg (Fluoxetine 10lbl)

FLUOXETINE 10 mg Capsules, USP label from Micro Labs Limited. The label states each capsule contains fluoxetine hydrochloride equivalent to 10 mg of fluoxetine. It includes storage instructions, dispensing information, and identifies the manufacturer as Micro Labs Limited, Goa, India, with manufacturing for Micro Labs USA, Inc. The package contains 30 capsules.*

FDA Label Image

Fluoxetine-20lbl.jpg (Fluoxetine 20lbl)

Label for Fluoxetine Capsules, USP 20 mg by Micro Labs Limited. The label includes dosage strength, NDC 42571-388-30, storage instructions to keep at controlled room temperature, and dispensing guidance. It indicates a 30-capsule package and notes manufacturing details for Micro Labs Limited, Goa, India, and Micro Labs USA, Inc., New Jersey.*

FDA Label Image

Fluoxetine-40lbl.jpg (Fluoxetine 40lbl)

Fluoxetine Capsules, USP 40 mg label from Micro Labs Limited. The label includes dosage details, storage instructions, and a barcode. It specifies a quantity of 30 capsules and notes that it is Rx only. Manufactured for Micro Labs USA, Inc., Somerset, NJ, with manufacturing site in Goa, India.*

FDA Label Image

Structure (Fluoxetine Structure)

Chemical structure diagram of Fluoxetine hydrochloride showing the molecular arrangement with trifluoromethyl, phenyl, and secondary amine groups linked via an ether and alkyl chain.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.